CA1239413A - Dioxasilepin and dioxasilocin stabilizers - Google Patents
Dioxasilepin and dioxasilocin stabilizersInfo
- Publication number
- CA1239413A CA1239413A CA000445019A CA445019A CA1239413A CA 1239413 A CA1239413 A CA 1239413A CA 000445019 A CA000445019 A CA 000445019A CA 445019 A CA445019 A CA 445019A CA 1239413 A CA1239413 A CA 1239413A
- Authority
- CA
- Canada
- Prior art keywords
- butyl
- tert
- tetra
- carbon atoms
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003381 stabilizer Substances 0.000 title abstract description 18
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910000077 silane Inorganic materials 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 32
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 230000000087 stabilizing effect Effects 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000011368 organic material Substances 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 125000001118 alkylidene group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 230000015556 catabolic process Effects 0.000 claims description 3
- 238000006731 degradation reaction Methods 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- CLQYRTUQXDCING-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-11-methylbenzo[d][1,3,6,2]benzodioxathiasilocine Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C(S2)C=C(C=C3C(C)(C)C)C(C)(C)C)C)C(=C1)C(C)(C)C CLQYRTUQXDCING-UHFFFAOYSA-N 0.000 claims 1
- ORIFTGSJNNFCRX-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-11-phenyl-5H-benzo[d][1,3,2]benzodioxasilocine Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C(C2)C=C(C=C3C(C)(C)C)C(C)(C)C)C3=CC=CC=C3)C(=C1)C(C)(C)C ORIFTGSJNNFCRX-UHFFFAOYSA-N 0.000 claims 1
- ZTXNKOLGGKMBQA-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-5,11,11-trimethyl-5h-benzo[d][1,3,2]benzodioxasilocine Chemical compound CC1C2=CC(C(C)(C)C)=CC(C(C)(C)C)=C2O[Si](C)(C)OC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C ZTXNKOLGGKMBQA-UHFFFAOYSA-N 0.000 claims 1
- QJMZXBIAZFOIAJ-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-5,11-dimethyl-5H-benzo[d][1,3,2]benzodioxasilocine Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C(C2C)C=C(C=C3C(C)(C)C)C(C)(C)C)C)C(=C1)C(C)(C)C QJMZXBIAZFOIAJ-UHFFFAOYSA-N 0.000 claims 1
- UYCBQJMMHNGWLZ-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-5H-benzo[d][1,3,2]benzodioxasilocine Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH2]OC3=C(C2)C=C(C=C3C(C)(C)C)C(C)(C)C)C(=C1)C(C)(C)C UYCBQJMMHNGWLZ-UHFFFAOYSA-N 0.000 claims 1
- VVRGTMMQOMGVQA-UHFFFAOYSA-N 2,4,8,10-tetratert-butyl-6,6-dimethylbenzo[d][1,3,2]benzodioxasilepine Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC2=C1O[Si](C)(C)OC1=C2C=C(C(C)(C)C)C=C1C(C)(C)C VVRGTMMQOMGVQA-UHFFFAOYSA-N 0.000 claims 1
- YBXHHKNHXWULBF-UHFFFAOYSA-N 2,4,8,10-tetratert-butyl-6-methylbenzo[d][1,3,2]benzodioxasilepine Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C2C=C(C=C3C(C)(C)C)C(C)(C)C)C)C(=C1)C(C)(C)C YBXHHKNHXWULBF-UHFFFAOYSA-N 0.000 claims 1
- ZQDJCOGIHUKXNW-UHFFFAOYSA-N C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C(S2)C=C(C=C3C(C)(C)C)C(C)(C)C)C3=CC=CC=C3)C(=C1)C(C)(C)C Chemical compound C(C)(C)(C)C1=CC2=C(O[SiH](OC3=C(S2)C=C(C=C3C(C)(C)C)C(C)(C)C)C3=CC=CC=C3)C(=C1)C(C)(C)C ZQDJCOGIHUKXNW-UHFFFAOYSA-N 0.000 claims 1
- 229920001059 synthetic polymer Polymers 0.000 claims 1
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- 150000004756 silanes Chemical class 0.000 abstract 2
- 239000000806 elastomer Substances 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
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- 229920000180 alkyd Polymers 0.000 description 9
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- 239000003963 antioxidant agent Substances 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
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- 239000000843 powder Substances 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- HXYXTCJDWHHCBW-UHFFFAOYSA-N acetonitrile;toluene Chemical compound CC#N.CC1=CC=CC=C1 HXYXTCJDWHHCBW-UHFFFAOYSA-N 0.000 description 4
- UWGIJJRGSGDBFJ-UHFFFAOYSA-N dichloromethylsilane Chemical compound [SiH3]C(Cl)Cl UWGIJJRGSGDBFJ-UHFFFAOYSA-N 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
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- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 3
- ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
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- 229920001971 elastomer Polymers 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
- 239000004611 light stabiliser Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
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- 229940116351 sebacate Drugs 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- FDGZUBKNYGBWHI-UHFFFAOYSA-N trioctadecyl phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC FDGZUBKNYGBWHI-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- OOZBTDPWFHJVEK-UHFFFAOYSA-N tris(2-nonylphenyl) phosphate Chemical compound CCCCCCCCCC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC OOZBTDPWFHJVEK-UHFFFAOYSA-N 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/549—Silicon-containing compounds containing silicon in a ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/04—Esters of silicic acids
- C07F7/07—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US457,349 | 1983-01-12 | ||
| US06/457,349 US4503243A (en) | 1983-01-12 | 1983-01-12 | Dioxasilepin and dioxasilocin stabilizers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1239413A true CA1239413A (en) | 1988-07-19 |
Family
ID=23816382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000445019A Expired CA1239413A (en) | 1983-01-12 | 1984-01-10 | Dioxasilepin and dioxasilocin stabilizers |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4503243A (de) |
| EP (1) | EP0114148B1 (de) |
| JP (1) | JPS59134799A (de) |
| CA (1) | CA1239413A (de) |
| DE (1) | DE3473877D1 (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4775497A (en) * | 1986-10-24 | 1988-10-04 | Ciba-Geigy Corporation | Esterification process with calcium hydroxyaryl phosphonate-organosilicon heterocycle catalyst system |
| GB0023089D0 (en) | 2000-09-20 | 2000-11-01 | Eastman Kodak Co | Photographic element dye-forming coupler and stabilizing compound |
| GB0127068D0 (en) * | 2001-11-10 | 2002-01-02 | Eastman Kodak Co | Photographic elements containing cyan coupler UV absorber and stabilizer |
| JP5592054B2 (ja) * | 2005-02-18 | 2014-09-17 | 日立化成株式会社 | 新規硬化性樹脂とその製造方法、及びエポキシ樹脂組成物、電子部品装置 |
| DE102009037236A1 (de) | 2009-08-12 | 2011-02-17 | Giesecke & Devrient Gmbh | Folienverbundbanknote und Verfahren zu ihrer Herstellung |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB798163A (en) * | 1953-12-05 | 1958-07-16 | Siemens Ag | Process for the production of ú´,ú´-diphenyldioxy silanes |
| BE553340A (de) * | 1956-03-17 | |||
| US2983745A (en) * | 1956-07-18 | 1961-05-09 | Dow Corning | Silpropoxanes |
| US2963502A (en) * | 1958-05-26 | 1960-12-06 | Ford Motor Co | Bis (2, 6-diisopropylphenoxy)-dimethylsilane |
| US3083219A (en) * | 1961-03-15 | 1963-03-26 | Gen Electric | Intercondensation of tetrahydrofuran with organohalosilanes |
| US3256308A (en) * | 1962-03-05 | 1966-06-14 | Dow Chemical Co | 2-methyl-1, 3-dioxa-2-sila-cyclohept-5-ene |
| DE1244183B (de) * | 1964-02-29 | 1967-07-13 | Dynamit Nobel Ag | Verfahren zur Herstellung von Aroxysilanen |
| SU467078A1 (ru) * | 1973-01-02 | 1975-04-15 | Предприятие П/Я Г-4236 | Способ получени дисиладиоксадибензоциклооктана |
| US4252967A (en) * | 1979-06-20 | 1981-02-24 | Stauffer Chemical Company | Dihaloneopentyl silicate flame retardants |
| US4447628A (en) * | 1982-07-12 | 1984-05-08 | E. I. Du Pont De Nemours And Company | Nonhygroscopic, anionic pentacoordinate silicate |
-
1983
- 1983-01-12 US US06/457,349 patent/US4503243A/en not_active Expired - Fee Related
-
1984
- 1984-01-06 EP EP84810007A patent/EP0114148B1/de not_active Expired
- 1984-01-06 DE DE8484810007T patent/DE3473877D1/de not_active Expired
- 1984-01-10 CA CA000445019A patent/CA1239413A/en not_active Expired
- 1984-01-12 JP JP59004213A patent/JPS59134799A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP0114148A2 (de) | 1984-07-25 |
| US4503243A (en) | 1985-03-05 |
| EP0114148B1 (de) | 1988-09-07 |
| EP0114148A3 (en) | 1985-12-27 |
| DE3473877D1 (de) | 1988-10-13 |
| JPH0460117B2 (de) | 1992-09-25 |
| JPS59134799A (ja) | 1984-08-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |